ClinVar Miner

List of variants studied for Warburg micro syndrome 3

Included ClinVar conditions (1):
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ClinVar version:
Total variants: 110
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HGVS dbSNP
NC_000010.11:g.27504220G>A
NM_001256410.1(RAB18):c.-144T>A rs780539442
NM_001256410.1(RAB18):c.-182G>A rs770568854
NM_001256410.1(RAB18):c.-79T>A rs886046964
NM_001256410.1(RAB18):c.-83C>A rs115326586
NM_021252.5(RAB18):c.*1041A>G
NM_021252.5(RAB18):c.*1047T>G
NM_021252.5(RAB18):c.*1089C>A rs189434439
NM_021252.5(RAB18):c.*1110A>G
NM_021252.5(RAB18):c.*1136G>A rs753649409
NM_021252.5(RAB18):c.*1141T>C rs751708158
NM_021252.5(RAB18):c.*1412C>T rs10508723
NM_021252.5(RAB18):c.*1452G>A
NM_021252.5(RAB18):c.*1488A>C rs148630305
NM_021252.5(RAB18):c.*1502G>C rs767488036
NM_021252.5(RAB18):c.*150C>A
NM_021252.5(RAB18):c.*1542T>C rs10508724
NM_021252.5(RAB18):c.*1589T>C
NM_021252.5(RAB18):c.*1680A>T rs886046972
NM_021252.5(RAB18):c.*1696T>A rs886046973
NM_021252.5(RAB18):c.*170T>C
NM_021252.5(RAB18):c.*1779A>T
NM_021252.5(RAB18):c.*1800A>G
NM_021252.5(RAB18):c.*1842A>G
NM_021252.5(RAB18):c.*1845G>T rs186064414
NM_021252.5(RAB18):c.*1895G>C rs746613469
NM_021252.5(RAB18):c.*1943G>A rs560571679
NM_021252.5(RAB18):c.*2085A>C
NM_021252.5(RAB18):c.*2242A>G rs186240753
NM_021252.5(RAB18):c.*2302A>G
NM_021252.5(RAB18):c.*2327T>C
NM_021252.5(RAB18):c.*2375A>G rs2477317
NM_021252.5(RAB18):c.*2420C>A rs770379811
NM_021252.5(RAB18):c.*2449A>G rs12260532
NM_021252.5(RAB18):c.*2476G>A rs12267298
NM_021252.5(RAB18):c.*2529G>A rs145293804
NM_021252.5(RAB18):c.*254A>G rs75899834
NM_021252.5(RAB18):c.*2744C>T rs12254670
NM_021252.5(RAB18):c.*2788C>T rs886046974
NM_021252.5(RAB18):c.*278A>T rs41282848
NM_021252.5(RAB18):c.*2862T>C rs767741672
NM_021252.5(RAB18):c.*2943A>G rs886046975
NM_021252.5(RAB18):c.*2974C>G rs532562164
NM_021252.5(RAB18):c.*2985T>G
NM_021252.5(RAB18):c.*3129C>T rs78270485
NM_021252.5(RAB18):c.*3166C>T rs886046977
NM_021252.5(RAB18):c.*3167G>A rs546186493
NM_021252.5(RAB18):c.*3193C>T rs886046978
NM_021252.5(RAB18):c.*3222C>T
NM_021252.5(RAB18):c.*3227A>G
NM_021252.5(RAB18):c.*325C>G rs886046970
NM_021252.5(RAB18):c.*3330G>C
NM_021252.5(RAB18):c.*3453G>A rs11015861
NM_021252.5(RAB18):c.*3476A>G rs11597728
NM_021252.5(RAB18):c.*3484T>C rs11598268
NM_021252.5(RAB18):c.*3521C>T
NM_021252.5(RAB18):c.*3543G>A
NM_021252.5(RAB18):c.*3559C>T rs117041769
NM_021252.5(RAB18):c.*3584C>T rs11015862
NM_021252.5(RAB18):c.*3696T>A rs10829269
NM_021252.5(RAB18):c.*3729G>C rs530960985
NM_021252.5(RAB18):c.*3766C>A
NM_021252.5(RAB18):c.*382C>T rs886046971
NM_021252.5(RAB18):c.*3832C>A
NM_021252.5(RAB18):c.*387C>A rs12248740
NM_021252.5(RAB18):c.*3906G>A
NM_021252.5(RAB18):c.*3927A>G rs886046981
NM_021252.5(RAB18):c.*3939A>T rs1047915
NM_021252.5(RAB18):c.*3967T>C
NM_021252.5(RAB18):c.*4008C>T
NM_021252.5(RAB18):c.*402T>C rs555933024
NM_021252.5(RAB18):c.*4038A>T
NM_021252.5(RAB18):c.*4039A>C rs886046982
NM_021252.5(RAB18):c.*407G>T
NM_021252.5(RAB18):c.*4131A>G
NM_021252.5(RAB18):c.*4185G>A
NM_021252.5(RAB18):c.*419G>A
NM_021252.5(RAB18):c.*448G>A
NM_021252.5(RAB18):c.*504A>G rs12571836
NM_021252.5(RAB18):c.*557G>A rs77758705
NM_021252.5(RAB18):c.*560C>T
NM_021252.5(RAB18):c.*62C>T rs886046969
NM_021252.5(RAB18):c.*635G>A
NM_021252.5(RAB18):c.*741A>G rs114899806
NM_021252.5(RAB18):c.*757G>T rs76051289
NM_021252.5(RAB18):c.*758A>T rs10508722
NM_021252.5(RAB18):c.*764A>G rs749045175
NM_021252.5(RAB18):c.*822T>C
NM_021252.5(RAB18):c.*890G>A rs539207601
NM_021252.5(RAB18):c.*8G>A
NM_021252.5(RAB18):c.*906A>G
NM_021252.5(RAB18):c.*946G>T
NM_021252.5(RAB18):c.*956A>C rs770434733
NM_021252.5(RAB18):c.*992C>A rs763254596
NM_021252.5(RAB18):c.*99C>T rs767920219
NM_021252.5(RAB18):c.-20C>T rs74127323
NM_021252.5(RAB18):c.-41A>G rs770276006
NM_021252.5(RAB18):c.270C>A (p.Val90=) rs750139202
NM_021252.5(RAB18):c.274_276AGA[1] (p.Arg93del) rs587776875
NM_021252.5(RAB18):c.284C>G (p.Thr95Arg) rs587777151
NM_021252.5(RAB18):c.298G>C (p.Asp100His) rs748274360
NM_021252.5(RAB18):c.36C>A (p.Leu12=) rs61757825
NM_021252.5(RAB18):c.394G>T (p.Asp132Tyr) rs190213580
NM_021252.5(RAB18):c.422G>A (p.Arg141Gln)
NM_021252.5(RAB18):c.454G>A (p.Ala152Thr) rs886046967
NM_021252.5(RAB18):c.592G>A (p.Ala198Thr) rs11015859
NM_021252.5(RAB18):c.619T>C (p.Ter207Gln) rs387906833
NM_021252.5(RAB18):c.68+10A>G rs886046965
NM_021252.5(RAB18):c.71T>A (p.Leu24Gln) rs387906832
RAB18, EX2DEL

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